Disease: Attention deficit hyperactivity disorder
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11789399
LOC105376249
0.882 0.040 9 118597008 intergenic variant G/A;C snv 5
rs12443954 0.851 0.040 16 89675088 intron variant A/C;G snv 5
rs1344706
ZNF804A
0.701 0.160 2 184913701 intron variant A/C;T snv 21
rs1412005 0.925 0.040 9 90646879 upstream gene variant T/A;G snv 3
rs2535629
ITIH3
0.827 0.040 3 52799203 intron variant G/A;C snv 9
rs2721800
MPP6
0.851 0.040 7 24652933 intron variant G/A;C;T snv 5
rs3749034
GAD1
0.827 0.040 2 170816965 5 prime UTR variant G/A;T snv 6
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs56037433
SLC4A10
0.925 0.040 2 161719475 intron variant G/A;T snv 2
rs5742905
CBS
0.701 0.360 21 43063074 missense variant A/G snv 22
rs58502974
ADCY2
0.925 0.040 5 7755787 intron variant T/A;G snv 2
rs6318
HTR2C ; LOC105373313
0.623 0.520 X 114731326 missense variant C/G;T snv 42
rs759834365
BDNF-AS ; BDNF
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs779867
GRM7
0.776 0.120 3 7442784 intron variant T/C;G snv 9
rs9297357
ZFPM2 ; LOC105375695
0.851 0.040 8 105130105 intron variant C/G;T snv 5
rs9951150 0.851 0.040 18 55153893 intergenic variant A/G;T snv 5
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1460808228
PRKCB
0.851 0.040 16 24185518 missense variant T/C snv 7.0E-06 4
rs1715
ZNF615
0.851 0.040 19 51991525 3 prime UTR variant T/C snv 1.4E-05 5
rs28364997
SLC6A3
0.807 0.120 5 1403013 missense variant G/A snv 5.3E-04 5.8E-04 9
rs1801028
DRD2
0.716 0.200 11 113412762 missense variant G/C snv 2.7E-02 1.8E-02 24
rs34096808
NLGN1
0.925 0.040 3 173822316 intron variant C/T snv 3.1E-02 2
rs36030485
LOC101930053 ; LOC105375956
0.925 0.040 9 2411646 TF binding site variant C/T snv 3.5E-02 2
rs8321
ZNRD1
0.742 0.320 6 30064745 3 prime UTR variant A/C snv 5.4E-02 5.9E-02 16
rs17662626
LOC107985969
0.851 0.040 2 193119895 intergenic variant A/G snv 5.9E-02 5